FDA NDC Directory · JSON-LD · Markdown
NDC 76045-216 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION
| Generic name | ONDANSETRON HYDROCHLORIDE |
|---|---|
| Labeler / Manufacturer | Fresenius Kabi USA, LLC |
| Marketing category | Abbreviated NDA (generic) · App ANDA202253 |
| Dosage form / route | INJECTION, SOLUTION · INTRAMUSCULAR INTRAVENOUS |
| Active ingredients | ONDANSETRON HYDROCHLORIDE (4 mg/2mL) |
| Marketing started | 20220531 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).